AutoRL framework for bioprocess control: Optimizing reward function, architecture, and hyperparameters
This study proposes a structured AutoRL framework for the development of deep reinforcement learning (DRL) controllers in chemical process systems. Focusing on the control of a 3 × 3 MIMO yeast fermentation bioreactor, the methodology jointly optimizes three key internal components of the DRL agent: the reward function, the neural network architecture, and the hyperparameters of the algorithm. A parameterizable logistic reward formulation is introduced to encode control objectives, such as steady-state accuracy, minimalization of actuation effort, and control smoothness, into a flexible and tunable structure. A dual loop optimization strategy combines grid search and Bayesian optimization to systematically explore and refine the agent’s design space. The resulting controller achieved average steady-state errors of 0.009 °C for reactor temperature and 0.19 g/L for ethanol concentration, while maintaining smooth and stable behavior under diverse operational scenarios. By formalizing reward design and integrating it with hyperparameter and architecture optimization, this work delivers a AutoRL methodology for DRL-based control, reducing reliance on expert heuristics and enhancing reproducibility in complex bioprocess applications. • AutoRL framework structured for process controller design. • Joint optimization of reward, architecture, and hyperparameters applied. • Parameterizable reward function enables interpretable alignment with control goals. • Validated on 3 × 3 MIMO yeast fermentation bioreactor with high precision. • AutoRL reduces expert dependency and enables scalable DRL in process control.
Institutions
- Universidade Federal do Rio Grande (BR)
- Universidade Estadual de Campinas (UNICAMP) (BR)
- University of Rio Grande and Rio Grande Community College (US)
Publication Details
- Journal
- Digital Chemical Engineering
- Published
- 2025-08-15
- DOI
- https://doi.org/10.1016/j.dche.2025.100261
- Citations
- 1
- Primary Topic
- Prenatal Screening and Diagnostics
- Type
- article
- Field-Weighted Citation Impact
- 3.49